Volume 26, Number 6 (2000), in the article “A New Exon 9 Glucose-6-phosphate Dehydrogenase Mutation (G6PD “Rehovot”) in a Jewish Ethiopian Family with Variable Phenotypes,” by Mona Iancovici-Kidon, Daliah Sthoeger, Ayala Abrahamov, Baruch Volach, Ernest Beutler, Terri Gelbart, and Yigal Barak, pages 567–571 (doi:10.1006/bcmd.2000.0334)

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Severe Jaundice in a Patient with a Previously Undescribed Glucose-6-phosphate Dehydrogenase (G6PD) Mutation and Gilbert Syndrome

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